SCHEMBL6137196

SCHEMBL6137196

COC(=O)[C@H](C)NC(C)(C)C

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA14 Q9ULX7 3/20 0.50
CA12 O43570 2/20 0.44
SLC6A3 Q01959 5/20 0.42
SMN1; SMN2 Q16637 3/20 0.42
SLC6A2 P23975 5/20 0.39
CHRNA1 P02708 4/20 0.39
CHRNG P07510 4/20 0.39
CHRNB1 P11230 4/20 0.39
CHRNB2 P17787 4/20 0.39
CHRNB4 P30926 4/20 0.39
CHRNA3 P32297 4/20 0.39
CHRNA4 P43681 4/20 0.39
CHRND Q07001 4/20 0.39
SLC6A4 P31645 3/20 0.38
ITGA5 P08648 1/20 0.38
CYP2C19 P33261 1/20 0.38
HRH1 P35367 1/20 0.38
CHRNA7 P36544 1/20 0.38
OPRK1 P41145 1/20 0.38
KCNH2 Q12809 1/20 0.38

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL13646104 1.00 CA14 (0.50) CA14CA12SLC6A3SMN1; SMN2SLC6A2
SCHEMBL13166671 1.00 CA14 (0.50) CA14CA12SLC6A3SMN1; SMN2SLC6A2
SCHEMBL15837231 0.83 SLC6A3 (0.39) CA14CA12SLC6A3SMN1; SMN2SLC6A2
SCHEMBL15497667 0.83 SLC6A3 (0.39) CA14CA12SLC6A3SMN1; SMN2SLC6A2
SCHEMBL11186119 0.81 METAP2 (0.43) SLC6A3SLC6A2CHRNA1CHRNGCHRNB1
SCHEMBL7857076 0.81 METAP2 (0.43) SLC6A3SLC6A2CHRNA1CHRNGCHRNB1
SCHEMBL18430098 0.81 CA14 (0.35) CA14CA12SLC6A3SMN1; SMN2SLC6A2
SCHEMBL15497665 0.80 SLC6A3 (0.37) CA14CA12SLC6A3SMN1; SMN2SLC6A2
SCHEMBL20329438 0.80 CA14 (0.42) CA14CA12SMN1; SMN2ALDH1A1CA1
SCHEMBL17403508 0.79 SLC6A3 (0.42) CA14CA12SLC6A3SMN1; SMN2SLC6A2

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 14 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2021250531-A1 4-(4,5-DIHYDRO-1H-PYRAZOL-1-YL)PYRIMIDINE COMPOUND AS CANNABINOID RECEPTOR (CB1 RECEPTOR) ANTAGONISTS AND PHARMACEUTICAL COMPOSITION INCLUDING SAME 주식회사 종근당 2021-12-16 WO disclosed
US-10208035-B2 Compounds for inhibiting drug-resistant strains of HIV-1 integrase THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 2019-02-19 US disclosed
US-20170305904-A1 COMPOUNDS FOR INHIBITING DRUG-RESISTANT STRAINS OF HIV-1 INTEGRASE THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERV (US) 2017-10-26 US disclosed
US-9676771-B2 Compounds for inhibiting drug-resistant strains of HIV-1 integrase THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 2017-06-13 US disclosed
US-7649015-B2 Cellular accumulation of phosphonate analogs of HIV protease inhibitor compounds GILEAD SCIENCES, INC. (US) 2010-01-19 US disclosed
US-7507820-B2 Diazaphosphacycles WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 2009-03-24 US disclosed
US-20070190523-A1 Method and compositions for identifying anti-hiv therapeutic compounds GILEAD SCIENCES, INC. 2007-08-16 US disclosed
US-20070190523-A1 Method and compositions for identifying anti-hiv therapeutic compounds GILEAD SCIENCES, INC. 2007-08-16 US disclosed
US-20070010489-A1 Cellular accumulation of phosphonate analogs of hiv protease inhibitor compounds GILEAD SCIENCES, INC. 2007-01-11 US disclosed
EP-1255542-A4 SUBSTITUTED AMINO ACIDS AS NEUTRAL SPHINGOMYELINASE INHIBITORS ORTHO MCNEIL PHARM INC (US) 2005-02-02 EP disclosed
EP-1255542-A1 SUBSTITUTED AMINO ACIDS AS NEUTRAL SPHINGOMYELINASE INHIBITORS Ortho-Mcneil Pharmaceutical, Inc. (US) 2002-11-13 EP disclosed
US-6306911-B1 ENZYME INHIBITORS ORTHO-MCNEIL PHARMACEUTICAL, INC. 2001-10-23 US disclosed
WO-2001056560-A1 SUBSTITUTED AMINO ACIDS AS NEUTRAL SPHINGOMYELINASE INHIBITORS ORTHO-MCNEIL PHARMACEUTICAL, INC. (US) 2001-08-09 WO disclosed
US-6114310-A THERAPY FOR MICROBIAL INFECTIONS MICROCIDE PHARMACEUTICALS, INC. (US) 2000-09-05 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (3 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-10208035-B2 Compounds for inhibiting drug-resistant strains of HIV-1 integrase CCR8, CDK8, CHD8 CA14 3863/4885CA12 4127/4885SLC6A3 2108/4885
US-20170305904-A1 COMPOUNDS FOR INHIBITING DRUG-RESISTANT STRAINS OF HIV-1 INTEGRASE CCR8, CDK8, CHD8 CA14 3863/4885CA12 4127/4885SLC6A3 2108/4885
US-20070010489-A1 Cellular accumulation of phosphonate analogs of hiv protease inhibitor compounds PPA1, PNP, PPME1 CA14 3387/4885CA12 4301/4885SLC6A3 3259/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.